Improving Future Thinking Among Mothers

Parent-Child Memory Study: Improving Future Thinking Among Mothers From a Traditionally Underserved Community to Reduce Harsh Parenting and Improve Child Outcomes - A Randomized Controlled Trial

Not applicable Interventional Henry Ford Health System · NCT06145919

This study is testing a new way to help mothers from low-resource communities think more about the future to see if it can improve their parenting and strengthen their relationship with their children.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment144 (estimated)
Ages5 Years and up
SexFemale
SponsorHenry Ford Health System Academic / other
Locations1 site (Flint, Michigan)
Trial IDNCT06145919 on ClinicalTrials.gov

What this trial studies

This study focuses on mothers from low-resource communities and aims to reduce harsh parenting practices linked to mental health issues in children. It will implement a brief intervention targeting maternal delay discounting, which is the tendency to prioritize immediate rewards over long-term benefits. Participants will be randomly assigned to either an Episodic Future Thinking (EFT) or an Episodic Recent Thinking (ERT) intervention. The effectiveness of these interventions will be evaluated in terms of their impact on parenting behaviors and the parent-child relationship.

Who should consider this trial

Good fit: Ideal candidates are mothers or grandmothers from the Flint area with children aged 5-10 who are willing to participate in the study.

Not a fit: Patients with active suicidality, severe mental health disorders, or current involvement with child protective services may not benefit from this study.

Why it matters

Potential benefit: If successful, this intervention could lead to improved parenting practices and better mental health outcomes for children in underserved communities.

How similar studies have performed: While similar interventions targeting parenting behaviors have shown promise, this specific approach focusing on delay discounting in low-resource settings is relatively novel.

Eligibility criteria

Show full inclusion / exclusion criteria
Parent Inclusion Criteria:

1. A mother and or grandmother from the Flint area with a child/grandchild between the ages of 5-10 who can provide legal consent for that child
2. Self-report that they have consistent contact with the child/grandchild
3. Willing to participate in the study
4. Able to participate in written assessments and an intervention conducted in English
5. Have a working cell phone that can receive and send text messages and be willing to receive/send text messages as part of the study
6. Have a phone or device that's able to use video conferencing software if interested in virtual participation

Parent Exclusion Criteria:

1. Self-disclosed active suicidality/homicidality
2. Self-disclosed current bipolar disorder, schizophrenia, or psychosis
3. Self-reported current and ongoing involvement with child protective services

Child Inclusion Criteria:

1. Children must be between the ages of 5-10 and have a mother/grandmother willing to provide consent for their participation
2. Willing to participate in parent-child observation sessions
3. Elementary proficiency in English
4. Willing to participate in study surveys

Child Exclusion criteria:

1. Self-disclosed active suicidality/homicidality
2. Self-disclosed current bipolar disorder, schizophrenia, or psychosis

Where this trial is running

Flint, Michigan

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Behavior, Healthepisodic future thinkingepisodic recent thinkingdelay discountingparent-child relationslow resourceFlint, Michiganspecial play time
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.